US9895380B2ActiveUtilityA1
Methods and pharmaceutical compositions for the treatment of hepatitis B virus infection
Est. expirySep 11, 2033(~7.2 yrs left)· nominal 20-yr term from priority
Inventors:Patrice AndreVincent LotteauPauline RadreauMarine GilardoneAmaury PatinDidier RocheDaniel CravoSophie Hallakou-Bozec
A61P 43/00A61P 31/20A61P 1/16A61P 1/00A61K 31/551A61K 31/42A61K 31/55A61K 31/496A61K 31/522A61K 31/4525A61K 31/513A61K 38/212A61K 31/675A61K 31/7072A61K 45/06A61K 31/575A61K 2300/00
80
PatentIndex Score
5
Cited by
14
References
9
Claims
Abstract
The present invention relates to methods and pharmaceutical compositions for the treatment of hepatitis B virus infection. In particular, the present invention relates to farnesoid X receptor (FXR) agonists for use in a method for the treatment of hepatitis B virus infection in a subject in need thereof.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. A method for reducing hepatitis B virus (HBV) replication in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a farnesoid X receptor (FXR) antagonist.
2. The method of claim 1 , wherein the subject is infected with a hepatitis B virus genotype selected from A, B, C, and D.
3. The method of claim 1 , wherein the subject has a chronic HBV infection.
4. The method of claim 1 , wherein the farnesoid X receptor (FXR) agonist is a selective FXR agonist.
5. The method of claim 1 , wherein the farnesoid X receptor (FXR) agonist is selected from the group consisting of the compounds identified by the CAS REGISTRY NUMBERS 1192171-69-9, 6ECDCA, GW4064, PXL0914, and PXL0743.
6. The method of claim 1 , wherein the farnesoid X receptor (FXR) agonist is selected from the group consisting of the compounds identified by the CAS REGISTRY NUMBERS 1192171-69-9 and 6ECDCA.
7. The method of claim 1 , wherein the subject has failed to respond to a previous treatment for HBV infection.
8. The method of claim 7 , wherein the previous treatment is selected from the group consisting of lamivudine (Epivir), adefovir (Hepsera), tenofovir (Viread), telbivudine (Tyzeka), entecavir (Baraclude), interferon alpha-2a, PEGylated interferon alpha-2a (Pegasys) and interferon alpha-2b (ViraferonPeg or Introna).
9. The method of claim 1 , wherein the FXR agonist is administered in combination with a treatment selected from the group consisting of lamivudine (Epivir), adefovir (Hepsera), tenofovir (Viread), telbivudine (Tyzeka), entecavir (Baraclude), interferon alpha-2a, PEGylated interferon alpha-2a (Pegasys) and interferon alpha-2b (ViraferonPeg or Introna).Cited by (0)
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